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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5831296copy number variation2nstd209human GRCh38 chr2: 131,532,325-131,534,118 , GRCh37.p13 chr2: 132,289,898-132,291,691 CCDC74A, MED15P4
    nsv5665937inversion1nstd207human GRCh38 chr2: 130,138,213-131,531,319 , GRCh37.p13 chr2: 130,895,786-132,288,892 , GNAQP1, 84 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5439461copy number variation1nstd206human GRCh38 chr2: 131,381,309-131,531,618 , GRCh37.p13 chr2: 132,138,882-132,289,191 MTCO2P18, LOC112268425, 17 more genes
    nsv5437602copy number variation1nstd206human GRCh38 chr2: 131,208,309-131,740,809 , GRCh37.p13 chr2: 131,965,882-132,498,382 , LINC01120, 42 more genes
    nsv5434881copy number variation1nstd206human GRCh38 chr2: 131,531,618-131,544,000 , GRCh37.p13 chr2: 132,289,191-132,301,573 CCDC74A, MED15P4
    nsv5434286copy number variation1nstd206human GRCh38 chr2: 131,208,118-131,540,100 , GRCh37.p13 chr2: 131,965,691-132,297,673 , MTND2P18, 35 more genes
    nsv5220357copy number variation1nstd204human GRCh38.p13 chr2: 131,532,920-131,534,418 , GRCh37.p13 chr2: 132,290,493-132,291,991 CCDC74A, MED15P4
    nsv5209396copy number variation1nstd204human GRCh38.p13 chr2: 131,533,001-131,534,400 , GRCh37.p13 chr2: 132,290,574-132,291,973 CCDC74A, MED15P4
    nsv5203847copy number variation1nstd204human GRCh38.p13 chr2: 131,532,820-131,545,434 , GRCh37.p13 chr2: 132,290,393-132,303,007 CCDC74A, MED15P4
    nsv5200953copy number variation1nstd204human GRCh38.p13 chr2: 131,532,325-131,541,463 , GRCh37.p13 chr2: 132,289,898-132,299,036 CCDC74A, MED15P4
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4926075copy number variation1nstd200human GRCh38 chr2: 130,830,344-131,824,388 , GRCh37.p13 chr2: 131,587,917-132,581,961 , LOC112268425, 50 more genes
    nsv4923974copy number variation1nstd200human GRCh38 chr2: 131,099,303-132,437,777 , GRCh37.p13 chr2: 131,856,876-133,195,350 , MTND4P21, 67 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4770868copy number variation1nstd200human GRCh37 chr2: 131,587,942-132,581,943 , GRCh38.p12 chr2: 130,830,369-131,824,370 , ARHGEF4, 50 more genes
    nsv4727950copy number variation1nstd197human GRCh38.p12 chr2: 131,532,865-131,533,069 , GRCh37 chr2: 132,290,438-132,290,642 CCDC74A, MED15P4
    nsv4684238copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 122,952,356-133,826,358 , GRCh38.p12 chr2: 122,194,780-133,068,785 BIN1, ERCC3, 211 more genes
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